ENST00000367698.4:c.1238A>T
MANE Select
|
ENSP00000356671.3:p.Glu413Val
|
|
ENST00000367698.3:c.1238A>T
|
ENSP00000356671.3:p.Glu413Val
|
|
ENST00000617423.4:c.623A>T
|
ENSP00000478688.1:p.Glu208Val
|
|
NM_000488.3:c.1238A>T , LRG_577t1:c.1238A>T
|
NP_000479.1:p.Glu413Val
|
|
XM_005245198.2:c.1094A>T
|
XP_005245255.1:p.Glu365Val
|
|
NM_001365052.1:c.1094A>T
|
NP_001351981.1:p.Glu365Val
|
|
NM_000488.4:c.1238A>T
MANE Select
|
NP_000479.1:p.Glu413Val
|
|
NM_001365052.2:c.1094A>T
|
NP_001351981.1:p.Glu365Val
|
|
NM_001386302.1:c.1361A>T
|
NP_001373231.1:p.Glu454Val
|
|
NM_001386303.1:c.1319A>T
|
NP_001373232.1:p.Glu440Val
|
|
NM_001386304.1:c.1217A>T
|
NP_001373233.1:p.Glu406Val
|
|
NM_001386305.1:c.1181A>T
|
NP_001373234.1:p.Glu394Val
|
|
NM_001386306.1:c.1022A>T
|
NP_001373235.1:p.Glu341Val
|
|